Trimethyl lock: a trigger for molecular release in chemistry, biology, and pharmacology

TitleTrimethyl lock: a trigger for molecular release in chemistry, biology, and pharmacology
Publication TypeJournal Article
Year of Publication2012
AuthorsLevine, MN, Raines, RT
JournalChemical Science
Volume3
Pagination2412-2420
Type of ArticleArticle
ISBN Number2041-6520
Accession NumberWOS:000305900700001
Keywordsalkaline-phosphatase, amine, antitumor agent, delivery, hydroxy amide lactonization, intramolecular conjugate addition, latent fluorophore, peptide-bond, prodrugs, rate enhancement, rstmann b, 1985, journal of immunological methods, v79, p27, stereopopulation-control, systems
Abstract

The trimethyl lock is an o-hydroxydihydrocinnamic acid derivative in which unfavorable steric interactions between three pendant methyl groups encourage lactonization to form a hydrocoumarin. This reaction is extremely rapid, even when the electrophile is an amide and the leaving group is an amino group of a small-molecule drug, fluorophore, peptide, or nucleic acid. O-Acylation of the phenolic hydroxyl group prevents reaction, providing a trigger for the reaction. Thus, the release of an amino group from an amide can be coupled to the hydrolysis of a designated ester (or to another chemical reaction that regenerates the hydroxyl group). Trimethyl lock conjugates are easy to synthesize, making the trimethyl lock a highly versatile module for chemical biology and related fields.